6A8G
| The crystal structure of muPAin-1-IG in complex with muPA-SPD at pH8.5 | 分子名称: | PHOSPHATE ION, Urokinase-type plasminogen activator chain B, muPAin-1-IG | 著者 | Wang, D, Yang, Y.S, Jiang, L.G, Huang, M.D, Li, J.Y, Andreasen, P.A, Xu, P, Chen, Z. | 登録日 | 2018-07-08 | 公開日 | 2019-02-20 | 最終更新日 | 2023-11-22 | 実験手法 | X-RAY DIFFRACTION (2.53 Å) | 主引用文献 | Suppression of Tumor Growth and Metastases by Targeted Intervention in Urokinase Activity with Cyclic Peptides. J.Med.Chem., 62, 2019
|
|
6A8N
| The crystal structure of muPAin-1-IG-2 in complex with muPA-SPD at pH8.5 | 分子名称: | CYS-PRO-ALA-TYR-SER-ARG-TYR-ILE-GLY-CYS, Urokinase-type plasminogen activator B | 著者 | Wang, D, Yang, Y.S, Jiang, L.G, Huang, M.D, Li, J.Y, Andreasen, P.A, Xu, P, Chen, Z. | 登録日 | 2018-07-09 | 公開日 | 2019-02-20 | 最終更新日 | 2023-11-22 | 実験手法 | X-RAY DIFFRACTION (2.489 Å) | 主引用文献 | Suppression of Tumor Growth and Metastases by Targeted Intervention in Urokinase Activity with Cyclic Peptides. J.Med.Chem., 62, 2019
|
|
7MEM
| |
3D27
| E. coli methionine aminopeptidase with Fe inhibitor W29 | 分子名称: | 4-(3-ethylthiophen-2-yl)benzene-1,2-diol, MANGANESE (II) ION, Methionine aminopeptidase | 著者 | Ye, Q.Z, Chai, S, He, H.Z. | 登録日 | 2008-05-07 | 公開日 | 2008-08-19 | 最終更新日 | 2024-02-21 | 実験手法 | X-RAY DIFFRACTION (2.2 Å) | 主引用文献 | Discovery of inhibitors of Escherichia coli methionine aminopeptidase with the Fe(II)-form selectivity and antibacterial activity. J.Med.Chem., 51, 2008
|
|
3H0H
| |
3HNB
| |
3HOB
| |
8HJA
| The crystal structure of syn_CdgR-(c-di-GMP) from Synechocystis sp. PCC 6803 | 分子名称: | 9,9'-[(2R,3R,3aS,5S,7aR,9R,10R,10aS,12S,14aR)-3,5,10,12-tetrahydroxy-5,12-dioxidooctahydro-2H,7H-difuro[3,2-d:3',2'-j][1,3,7,9,2,8]tetraoxadiphosphacyclododecine-2,9-diyl]bis(2-amino-1,9-dihydro-6H-purin-6-one), c-di-GMP receptor | 著者 | Zeng, X, Peng, Y.J. | 登録日 | 2022-11-22 | 公開日 | 2023-03-29 | 実験手法 | X-RAY DIFFRACTION (2.38 Å) | 主引用文献 | A c-di-GMP binding effector controls cell size in a cyanobacterium. Proc.Natl.Acad.Sci.USA, 120, 2023
|
|
3HNY
| |
3H0F
| Crystal structure of the human Fyn SH3 R96W mutant | 分子名称: | 1-METHOXY-2-[2-(2-METHOXY-ETHOXY]-ETHANE, Proto-oncogene tyrosine-protein kinase Fyn | 著者 | Ponchon, L, Hoh, F, Labesse, G, Dumas, C, Arold, S.T. | 登録日 | 2009-04-09 | 公開日 | 2010-04-21 | 最終更新日 | 2023-11-01 | 実験手法 | X-RAY DIFFRACTION (2.61 Å) | 主引用文献 | Synergy and allostery in ligand binding by HIV-1 Nef. Biochem.J., 478, 2021
|
|
3H0I
| |
1LDP
| |
5WQ6
| |
5WPZ
| |
4O03
| Crystal structure of Ca2+ bound prothrombin deletion mutant residues 146-167 | 分子名称: | 2-acetamido-2-deoxy-beta-D-glucopyranose, CALCIUM ION, Prothrombin | 著者 | Pozzi, N, Chen, Z, Shropshire, D.B, Pelc, L.A, Di Cera, E. | 登録日 | 2013-12-13 | 公開日 | 2014-05-21 | 最終更新日 | 2023-12-06 | 実験手法 | X-RAY DIFFRACTION (3.38 Å) | 主引用文献 | The linker connecting the two kringles plays a key role in prothrombin activation. Proc.Natl.Acad.Sci.USA, 111, 2014
|
|
2NB7
| |
2NB8
| |
4D8D
| |
6ITE
| Crystal structure of group A Streptococcal surface dehydrogenase (SDH) | 分子名称: | Glyceraldehyde-3-phosphate dehydrogenase, NICOTINAMIDE-ADENINE-DINUCLEOTIDE, SULFATE ION | 著者 | Yuan, C, Li, R, Huang, M.D. | 登録日 | 2018-11-21 | 公開日 | 2019-09-25 | 最終更新日 | 2023-11-22 | 実験手法 | X-RAY DIFFRACTION (1.739 Å) | 主引用文献 | Structural determination of group A Streptococcal surface dehydrogenase and characterization of its interaction with urokinase-type plasminogen activator receptor. Biochem.Biophys.Res.Commun., 510, 2019
|
|
5F4H
| Archael RuvB-like Holiday junction helicase | 分子名称: | 1,2-ETHANEDIOL, GLYCEROL, Nucleotide binding protein PINc | 著者 | Zhai, B, DuPrez, K.T, Doukov, T.I, Shen, Y, Fan, L. | 登録日 | 2015-12-03 | 公開日 | 2016-12-21 | 最終更新日 | 2017-11-01 | 実験手法 | X-RAY DIFFRACTION (2.699 Å) | 主引用文献 | Structure and Function of a Novel ATPase that Interacts with Holliday Junction Resolvase Hjc and Promotes Branch Migration. J. Mol. Biol., 429, 2017
|
|
6ISQ
| structure of Lipase mutant with oxided Cys-His-Asp catalytic triad | 分子名称: | 1,2-ETHANEDIOL, ACETATE ION, ISOPROPYL ALCOHOL, ... | 著者 | Cen, Y.X, Zhou, J.H, Wu, Q. | 登録日 | 2018-11-18 | 公開日 | 2019-07-24 | 最終更新日 | 2023-11-22 | 実験手法 | X-RAY DIFFRACTION (1.86 Å) | 主引用文献 | Artificial cysteine-lipases with high activity and altered catalytic mechanism created by laboratory evolution. Nat Commun, 10, 2019
|
|
6ISR
| structure of lipase mutant with Cys-His-Asp catalytic triad | 分子名称: | DI(HYDROXYETHYL)ETHER, Lipase B, NICKEL (II) ION, ... | 著者 | Cen, Y.X, Zhou, J.H, Wu, Q. | 登録日 | 2018-11-18 | 公開日 | 2019-07-24 | 最終更新日 | 2023-11-22 | 実験手法 | X-RAY DIFFRACTION (2.6 Å) | 主引用文献 | Artificial cysteine-lipases with high activity and altered catalytic mechanism created by laboratory evolution. Nat Commun, 10, 2019
|
|
6ISP
| structure of Candida antarctica Lipase B mutant | 分子名称: | CALCIUM ION, Lipase B, N,N-BIS(3-D-GLUCONAMIDOPROPYL)DEOXYCHOLAMIDE | 著者 | Cen, Y.X, Zhou, J.H, Wu, Q. | 登録日 | 2018-11-18 | 公開日 | 2019-07-24 | 最終更新日 | 2023-11-22 | 実験手法 | X-RAY DIFFRACTION (1.88 Å) | 主引用文献 | Artificial cysteine-lipases with high activity and altered catalytic mechanism created by laboratory evolution. Nat Commun, 10, 2019
|
|
5GMP
| Crystal structure of EGFR 696-1022 T790M in complex with XTF-262 | 分子名称: | Epidermal growth factor receptor, N-[3-[2-[[2-methoxy-4-(4-methylpiperazin-1-yl)phenyl]amino]-5-methyl-7-oxidanylidene-pyrido[2,3-d]pyrimidin-8-yl]phenyl]prop-2-enamide | 著者 | Yan, X.E, Yun, C.H. | 登録日 | 2016-07-14 | 公開日 | 2017-06-28 | 最終更新日 | 2023-11-08 | 実験手法 | X-RAY DIFFRACTION (2.797 Å) | 主引用文献 | A structure-guided optimization of pyrido[2,3-d]pyrimidin-7-ones as selective inhibitors of EGFR(L858R/T790M) mutant with improved pharmacokinetic properties. Eur J Med Chem, 126, 2017
|
|
5HDO
| |